نتایج جستجو برای: nickel catalyst

تعداد نتایج: 76389  

2017
Justinus A. Satrio Brent H. Shanks Thomas D. Wheelock

Future large-scale production of H2 for use as a clean fuel will likely depend upon gasifying coal or biomass followed by steam reforming the resulting gas mixture and separating the CO2 byproduct. The process of steam reforming and CO2 separation can be greatly simplified by utilizing a new material that combines a reforming catalyst with a sorbent for CO2. Such a material was prepared in the ...

Journal: :iranian journal of hydrogen & fuel cell 2015
nahid khandan mahmoud ziarati reza karkeabadi mohammad ali ghafouri roozbahani

steam reforming is one of the most important processes for producing hydrogen from hydrocarbon fuels such as lpg and has attracted much attention due to its high efficiency and economy. in this study, the lpg steam reforming reaction was investigated on nickel catalysts supported on four various zeolites (h-y, na-y, hzsm5 and ferrierite). the catalytic tests were performed in a tubular fixed be...

2012
Shinji Ohmori Kazuko Takahashi Mikiko Ikeda Toshihiko Ubuka

Raney nickel catalyst alone removes sulfur in reasonable yield from organic sulfur compounds, such as thiols, thioethers, disulfides, hemithioacetals, hemithioketals, diketals, thioamides, thiolesters, thiophenes, thioazoles, sulfoxides, sulfones, isothiocyanates, thioureas, and also organoselenium and tellurium compounds. This desulfurization reaction, therefore, has been used for the solution...

2016
Derek T. Ahneman Abigail G. Doyle

We describe the functionalization of α-amino C-H bonds with aryl halides using a combination of nickel and photoredox catalysis. This direct C-H, C-X coupling uses inexpensive and readily available starting materials to generate benzylic amines, an important class of bioactive molecules. Mechanistically, this method features the direct arylation of α-amino radicals mediated by a nickel catalyst...

2014
Xujun Liu Leilei Guan Xiaoniu Fu Yu Zhao Jiada Wu Ning Xu

Light-absorbing and electrically conductive binary CNx nanocone (CNNC) arrays have been fabricated using a glow discharge plasma-assisted reaction deposition method. The intact CNNCs with amorphous structure and central nickel-filled pipelines could be vertically and neatly grown on nickel-covered substrates according to the catalyst-leading mode. The morphologies and composition of the as-grow...

Journal: :Organic & biomolecular chemistry 2014
Mitsuhiro Wada Takahisa Murata Hideaki Oikawa Hiroki Oguri

While metal-promoted activation of tertiary alkyl halides often causes elimination and hydrodehalogenation, we have developed a nickel-catalyzed reductive dimerization that allows the generation of a potently reactive tertiary radical equivalent to form a very congested C(sp(3))-C(sp(3)) bond even below room temperature. The catalytic protocol is applicable to the dimerization of several pyrrol...

Journal: :Journal of the American Chemical Society 2002
Jun Terao Hideyuki Watanabe Aki Ikumi Hitoshi Kuniyasu Nobuaki Kambe

A new method for the cross-coupling reaction of Grignard reagents with alkyl chlorides, bromides, and tosylates has been developed by the use of a nickel catalyst in the presence of a diene as an additive. This reaction proceeds efficiently at 0-25 degrees C in THF using primary and secondary alkyl and aryl Grignard reagents. Nickel complexes bearing no phosphine ligands, such as NiCl2, Ni(acac...

Journal: :Molecules 2011
Stéphane Sengmany Erwan Le Gall Eric Léonel

A range of novel 4-amino-6-arylpyrimidines has been prepared under mild conditions by an electrochemical reductive cross-coupling between 4-amino-6-chloro-pyrimidines and functionalized aryl halides. The process, which employs a sacrificial iron anode in conjunction with a nickel(II) catalyst, allows the formation of coupling products in moderate to high yields.

Journal: :Chemical communications 2015
Weili Si Xuan Zhang Naoki Asao Yoshinori Yamamoto Tienan Jin

A new Ni-catalyzed direct 1,4-difunctionalization of [60]fullerene with various benzyl bromides has been developed. The use of a DMSO additive combined with a nickel catalyst is indispensable for the formation of 1,4-dibenzyl fullerenes with a variety of functional groups. The reaction proceeds through the formation of a fullerene monoradical species.

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